Evidence map›Paper›PMID 41410385›Full record

ArticleJournal of proteome research2026

A High-Resolution Subcellular Map of Proteins in Cells with Motile Cilia.

Filippa Bertilsson, Feria Hikmet, Jan N Hansen, Mathias Uhlén, Loren Méar, Cecilia Lindskog

Abstract read
In one paragraph

Article in Journal of proteome research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Functional Diversity and Emerging Roles of Human NME/NDPK Group II Proteins.International journal of molecular sciences · 2026
    Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Filippa BertilssonDepartment of Immunology, Genetics and Pathology, Cancer Precision Medicine Research Unit, Uppsala University, SE-751 85 Uppsala, Sweden.ORCID 0009-0004-4243-5739
Feria HikmetDepartment of Immunology, Genetics and Pathology, Cancer Precision Medicine Research Unit, Uppsala University, SE-751 85 Uppsala, Sweden.
Jan N HansenScience for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, 171 21 Stockholm, Sweden.
Mathias UhlénScience for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, 171 21 Stockholm, Sweden.
Loren MéarDepartment of Immunology, Genetics and Pathology, Cancer Precision Medicine Research Unit, Uppsala University, SE-751 85 Uppsala, Sweden.ORCID 0000-0001-9333-0110
Cecilia LindskogDepartment of Immunology, Genetics and Pathology, Cancer Precision Medicine Research Unit, Uppsala University, SE-751 85 Uppsala, Sweden.ORCID 0000-0001-5611-1015

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motile cilia are complex structures regulated by thousands of genes, essential for various physiological functions like respiration and reproduction. Their dysfunction can result in severe conditions like primary ciliary dyskinesia (PCD), highlighting the need for a deeper molecular understanding of their specific ciliary compartments. Interestingly, ciliated cells harbor multiple proteins with limited evidence on biological function, as defined by Functional Evidence (FE) scores, a grading system developed by the Human Proteome Project (HPP). Building upon the stringent antibody validation pipeline of the Human Protein Atlas (HPA) project, we developed a high-throughput workflow that combines a novel multiplex immunohistochemistry protocol with image analysis to investigate protein expression and subcellular localization in motile ciliated cells across five human tissues: nasopharynx, bronchus, fallopian tube, endometrium, and cervix. We spatially mapped >180 proteins, out of which 73% have FE scores 2-5, suggesting that further evidence is needed to establish these proteins' biological function. Notably, expression patterns varied between tissues, suggesting that motile cilia proteins are not universally expressed across the different epithelia. Our pipeline constitutes a promising resource for comprehensive mapping of the motile cilia proteome, and a first step toward identifying cilia proteins for functional studies to understand the molecular mechanisms underlying ciliopathies.

Indexed as

CiliaProteomeProteomicsBronchiCervix UteriFallopian TubesFemaleHumansImmunohistochemistryNasopharynxProteomeantibody-based proteomicsciliated cellshuman protein atlasimage analysismotile ciliamultiplex immunohistochemistryprotein mapping

Identifiers

PMID41410385
PMCPMC12772120

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.